Inhibitory synapse dysfunction and epileptic susceptibility associated with KIF2A deletion in cortical interneurons

Malformation of cortical development (MCD) is a family of neurodevelopmental disorders, which usually manifest with intellectual disability and early-life epileptic seizures. Mutations in genes encoding microtubules (MT) and MT-associated proteins are one of the most frequent causes of MCD in humans...

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Detalles Bibliográficos
Autores principales: Ruiz-Reig, Nuria, García-Sánchez, Dario, Schakman, Olivier, Gailly, Philippe, Tissir, Fadel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Molecular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887042/
https://www.ncbi.nlm.nih.gov/pubmed/36733270
http://dx.doi.org/10.3389/fnmol.2022.1110986

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887042/
https://www.ncbi.nlm.nih.gov/pubmed/36733270
http://dx.doi.org/10.3389/fnmol.2022.1110986

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